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nsv7058761

  • Variant Calls:1
  • Validation:Not tested
  • Clinical Assertions: No
  • Region Size:331,788

    Links to Other Resources

    Source: NCBI

    Genome View

    Select assembly:
    Overlapping variant regions from other studies: 942 SVs from 63 studies. See in: genome view    
    Submitted genomic12,041,264-12,373,051Question Mark
    Overlapping variant regions from other studies: 942 SVs from 63 studies. See in: genome view    
    Remapped(Score: Perfect):12,152,079-12,483,865Question Mark

    Variant Region Placement Information

    Variant Region IDPlacement TypeScoreAssemblyAssembly UnitReciprocitySequence IDChrStartStop
    nsv7058761Submitted genomicGRCh38 (hg38)Primary AssemblyNC_000019.10Chr1912,041,26412,373,051
    nsv7058761RemappedPerfectGRCh37.p13Primary AssemblyFirst PassNC_000019.9Chr1912,152,07912,483,865

    Variant Call Information

    Variant Call IDTypeMethodAnalysis
    nssv18757811inversionSequencingSplit read and paired-end mapping

    Variant Call Placement Information

    Variant Call IDPlacement TypeScoreHGVSAssemblyReciprocitySequence IDChrStartStop
    nssv18757811Submitted genomicNC_000019.10:g.120
    41264_12373051inv
    GRCh38 (hg38)NC_000019.10Chr1912,041,26412,373,051
    nssv18757811RemappedPerfectNC_000019.9:g.1215
    2079_12483865inv
    GRCh37.p13First PassNC_000019.9Chr1912,152,07912,483,865

    No validation data were submitted for this variant

    No clinical assertion data were submitted for this variant

    Complete genotype and/or allele frequency data for this study can be found on dbVar's FTP site.

    Genotype Information

    Variant Call IDAllele Frequency (AF)Allele Count (AC)Allele Number (AN)
    nssv187578114e-061276268
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